| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:44542828-44543044 | Common:1; Rare:39 | ||||
| chrX:46545380-46545530 | Rare:28 | ||||
| chrX:47144668-47144813 | Rare:24 | ||||
| chrX:47145089-47145338 | Rare:36 | ||||
| chrX:47232931-47233036 | Rare:26 | ||||
| chrX:47233283-47233456 | Rare:27 | ||||
| chrX:47482571-47482669 | Common:5; Rare:20; Clinvar:2 | ||||
| chrX:47483169-47483339 | Common:3; Rare:17 | ||||
| chrX:47836667-47836976 | Common:1; Rare:66 | ||||
| chrX:48003960-48004137 | Rare:48 | ||||
| chrX:48508880-48508999 | Rare:20 | ||||
| chrX:48696584-48696777 | Rare:43 | ||||
| chrX:48911637-48911706 | Rare:14; Clinvar (benign):3 | ||||
| chrX:48919013-48919271 | Rare:41 | ||||
| chrX:49073991-49074212 | Rare:52 |